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Completed Phase 4 Interventional Results available

Nebivolol in Patients With Systolic Stage 2 Hypertension

ClinicalTrials.gov ID: NCT01057251

Public ClinicalTrials.gov record NCT01057251. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 8:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Effect of 5 mg or 20 mg Nebivolol Once Daily on Blood Pressure in Patients With Systolic Stage 2 Hypertension

Study identification

NCT ID
NCT01057251
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Forest Laboratories
Industry
Enrollment
433 participants

Conditions and interventions

Conditions

Interventions

  • Nebivolol Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2010
Primary completion
Nov 30, 2010
Completion
Dec 31, 2010
Last update posted
Jan 10, 2012

2010 – 2011

United States locations

U.S. sites
36
U.S. states
17
U.S. cities
33
Facility City State ZIP Site status
Forest Investigative Site 008 Foley Alabama 36535
Forest Investigative Site 021 Montgomery Alabama 36117
Forest Investigative Site 006 Chino California 91710
Forest Investigative Site 002 Long Beach California 90806
Forest Investigative Site 004 Los Angeles California 90057
Forest Investigative Site 020 Temecula California 92591
Forest Investigative Site 028 Coral Gables Florida 33134
Forest Investigative Site 014 Daytona Beach Florida 32114
Forest Investigative Site 001 Fort Lauderdale Florida 33308
Forest Investigative Site 037 Fort Lauderdale Florida 33316
Forest Investigative Site 033 Hialeah Florida 33012
Forest Investigative Site 026 Jacksonville Florida 32216
Forest Investigative Site 017 Miami Florida 33133
Forest Investigative Site 010 Miami Florida 33169
Forest Investigative Site 030 Orlando Florida 32806
Forest Investigative Site 009 Atlanta Georgia 30338
Forest Investigative Site 031 Augusta Georgia 30904
Forest Investigative Site 039 Meridian Idaho 83646
Forest Investigative Site 007 Auburn Maine 04210
Forest Investigative Site 038 Baltimore Maryland 21204
Forest Investigative Site 011 Baltimore Maryland 21209
Forest Investigative Site 029 Prince Frederick Maryland 20678
Forest Investigative Site 023 Paw Paw Michigan 49079
Forest Investigative Site 005 Florissant Missouri 63033
Forest Investigative Site 041 Las Vegas Nevada 89106
Forest Investigative Site 040 New York New York 10010
Forest Investigative Site 012 Hickory North Carolina 28601
Forest Investigative Site 027 Salisbury North Carolina 28144
Forest Investigative Site 024 Harleysville Pennsylvania 19438
Forest Investigative Site 013 Charleston South Carolina 29407
Forest Investigative Site 035 Greenville South Carolina 29605
Forest Investigative Site 018 Mt. Pleasant South Carolina 29464
Forest Investigative Site 022 Simpsonville South Carolina 29681
Forest Investigative Site 003 Memphis Tennessee 38119
Forest Investigative Site 032 Corpus Christi Texas 78404
Forest Investigative Site 025 Richmond Virginia 23219

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01057251, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 10, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01057251 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →